1. Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes. Issue 1 (27th November 2014) Authors: Cady, Janet; Allred, Peggy; Bali, Taha; Pestronk, Alan; Goate, Alison; Miller, Timothy M.; Mitra, Robi D.; Ravits, John; Harms, Matthew B.; Baloh, Robert H. Journal: Annals of neurology Issue: Volume 77:Issue 1(2015:Jan.) Page Start: 100 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Dominant mutations in ITPR3 cause Charcot‐Marie‐Tooth disease. Issue 10 (19th September 2020) Authors: Rönkkö, Julius; Molchanova, Svetlana; Revah‐Politi, Anya; Pereira, Elaine M.; Auranen, Mari; Toppila, Jussi; Kvist, Jouni; Ludwig, Anastasia; Neumann, Julika; Bultynck, Geert; Humblet‐Baron, Stéphanie; Liston, Adrian; Paetau, Anders; Rivera, Claudio; Harms, Matthew B.; Tyynismaa, Henna; Ylikallio... Journal: Annals of clinical and translational neurology Issue: Volume 7:Issue 10(2020) Page Start: 1962 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Effects of mexiletine on hyperexcitability in sporadic amyotrophic lateral sclerosis: Preliminary findings from a small phase II randomized controlled trial. Issue 3 (31st December 2020) Authors: Weiss, Michael D.; Macklin, Eric A.; McIlduff, Courtney E.; Vucic, Steve; Wainger, Brian J.; Kiernan, Matthew C.; Goutman, Stephen A.; Goyal, Namita A.; Rutkove, Seward B.; Ladha, Shafeeq S.; Chen, I‐Hweii Amy; Harms, Matthew B.; Brannagan, Thomas H.; Lacomis, David; Zivkovic, Sasha; Ma, Maxwell;... Journal: Muscle & nerve Issue: Volume 63:Issue 3(2021) Page Start: 371 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetics of primary lateral sclerosis. (2nd November 2020) Authors: Silani, Vincenzo; Corcia, Philippe; Harms, Matthew B.; Rouleau, Guy; Siddique, Teepu; Ticozzi, Nicola Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 21(2020)Supplement 1 Page Start: 28 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Incorporating external information to improve sparse signal detection in rare‐variant gene‐set‐based analyses. Issue 4 (11th February 2020) Authors: Zhang, Mengqi; Gelfman, Sahar; McCarthy, Janice; Harms, Matthew B.; Moreno, Cristiane A.M.; Goldstein, David B.; Allen, Andrew S. Journal: Genetic epidemiology Issue: Volume 44:Issue 4(2020) Page Start: 330 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. MORC2 mutations cause axonal Charcot–Marie–Tooth disease with pyramidal signs. Issue 3 (13th January 2016) Authors: Albulym, Obaid M.; Kennerson, Marina L.; Harms, Matthew B.; Drew, Alexander P.; Siddell, Anna H.; Auer‐Grumbach, Michaela; Pestronk, Alan; Connolly, Anne; Baloh, Robert H.; Zuchner, Stephan; Reddel, Stephen W.; Nicholson, Garth A. Journal: Annals of neurology Issue: Volume 79:Issue 3(2016:Mar.) Page Start: 419 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Multifocal radiculoneuropathy during ipilimumab treatment of melanoma. Issue 3 (27th July 2013) Authors: Manousakis, Georgios; Koch, James; Sommerville, R. Brian; El‐Dokla, Ahmed; Harms, Matthew B.; Al‐Lozi, Muhammad T.; Schmidt, Robert E.; Pestronk, Alan Journal: Muscle & nerve Issue: Volume 48:Issue 3(2013:Sep.) Page Start: 440 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis. Issue 2 (27th January 2017) Authors: Güttsches, Anne‐Katrin; Brady, Stefen; Krause, Kathryn; Maerkens, Alexandra; Uszkoreit, Julian; Eisenacher, Martin; Schreiner, Anja; Galozzi, Sara; Mertens‐Rill, Janine; Tegenthoff, Martin; Holton, Janice L.; Harms, Matthew B.; Lloyd, Thomas E.; Vorgerd, Matthias; Weihl, Conrad C.; Marcus, Katrin... Journal: Annals of neurology Issue: Volume 81:Issue 2(2017) Page Start: 227 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗